Arthrex, Inc.
ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE
SKU K083707UPC HRX
In Stock
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IIFDA 510(k) Cleared (K083707)
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Free shipping on orders over $99 · 30-day returns
Arthrex, Inc.
Free shipping on orders over $99 · 30-day returns
ARTHREX DUAL WAVE ARTHROSCOPY FLUID MANAGEMENT DEVICE is an FDA 510(k)-cleared medical device (K083707) manufactured by Arthrex, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 2009. Regulation: 8.
